Canonical Allele Identifier: CA941623695

Gene: MMP1 WTAPP1

Linked Data

• dbSNP Id: rs1857986513
• gnomAD v3: 11-102790256-A-T
• gnomAD v4: 11-102790256-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790256A>T , CM000673.2:g.102790256A>T	GRCh38
NC_000011.9:g.102660987A>T , CM000673.1:g.102660987A>T	GRCh37
NC_000011.8:g.102166197A>T	NCBI36
NG_011740.1:g.12980T>A
NG_011740.2:g.12980T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.*156T>A (MMP1) MANE Select	ENSP00000322788.6:n.*156T>A
ENST00000680179.1:n.744T>A (MMP1)
ENST00000681445.1:n.740T>A (MMP1)
ENST00000681643.1:n.766T>A (MMP1)
ENST00000315274.6:c.*156T>A (MMP1)	ENSP00000322788.6:n.*156T>A
ENST00000371455.7:n.325-7768A>T (WTAPP1)
ENST00000525739.6:n.390-2889A>T (WTAPP1)
ENST00000544704.1:n.344+6192A>T (WTAPP1)
NM_001145938.1:c.*156T>A (MMP1)	NP_001139410.1:n.*156T>A
NM_002421.3:c.*156T>A (MMP1)	NP_002412.1:n.*156T>A
NR_038390.1:n.390-2889A>T (WTAPP1)
NM_002421.4:c.*156T>A (MMP1) MANE Select	NP_002412.1:n.*156T>A
NM_001145938.2:c.*156T>A (MMP1)	NP_001139410.1:n.*156T>A